Certivo

About

Certivo provides an electronic signature platform specifically engineered for regulated sectors such as clinical trials, pharmaceuticals, medical devices, and the broader life sciences. In contrast to generic e-signature solutions, Certivo's features are inherently designed to meet FDA 21 CFR Part 11 requirements. This includes ALCOA+ compliant audit trails featuring hash-chain verification, long-term document retention for 25 years, automated workflows, role-based access control, and integrated multi-factor authentication. Certivo is compliant with regulations including FDA, EU CTR 536/2014, MHRA 2026, and GDPR.